161 results · 29ms · Sources: EU EUDAMED, US FDA

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EEA 25MM SINGLE USE STAPLER WITH 3.5MM STAPLES

FDA Adverse Event
Death ·COVIDIEN, FORMERLY US SURGICAL A DIVISON·Product code GDW·April 25, 2016

EEA 25MM SINGLE-USE STAPLER

FDA Adverse Event
Death ·COVIDIEN, FORMERLY USSC PUERTO RICO INC·Product code GDW·April 25, 2016

VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT

FDA Adverse Event
Death ·ETHICON INC.·Product code GAM·July 7, 2022

PDS II POLYDIOXANONE SUTURE UNKNOWN PRODUCT

FDA Adverse Event
Death ·ETHICON INC.·Product code NEW·July 7, 2022

HARMONIC ACE 5MM SHEAR

FDA Adverse Event
Death ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·July 18, 2022

UNKNOWN EEA

FDA Adverse Event
Death ·US SURGICAL PUERTO RICO·Product code GDW·March 14, 2019

EEA ORVIL

FDA Adverse Event
Death ·COVIDIEN LP LLC NORTH HAVEN·Product code GDW·March 14, 2019

EEA

FDA Adverse Event
Death ·US SURGICAL PUERTO RICO·Product code GDW·March 19, 2019

ENDO STITCH

FDA Adverse Event
Death ·DAVIS & GECK CARIBE LTD·Product code OCW·March 19, 2019

UNKNOWN VLOC ENDO STITCH RELOAD ABS

FDA Adverse Event
Death ·COVIDIEN LP LLC NORTH HAVEN·Product code GAM·March 14, 2019

PDS II POLYDIOXANONE SUTURE UNKNOWN PRODUCT

FDA Adverse Event
Death ·ETHICON INC.·Product code NEW·October 25, 2022

QDOT MICRO

FDA Adverse Event
Death ·BIOSENSE WEBSTER INC·Product code OAE·October 23, 2024

NGEN GENERATOR

FDA Adverse Event
Death ·BIOSENSE WEBSTER INC·Product code OAE·October 23, 2024

HARMONIC ACE 5MM SHEAR

FDA Adverse Event
Death ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·November 8, 2022

PULMONARY VALVE & CONDUIT SG

FDA Adverse Event
Death ·CRYOLIFE, INC.·Product code MIE·January 5, 2012

PULMONARY VALVE & CONDUIT SG

FDA Adverse Event
Death ·CRYOLIFE, INC.·Product code MIE·January 17, 2012

LIFENET

FDA Adverse Event
Death ·LIFENET·Product code MIE·July 10, 1996

AORTIC VALVE & CONDUIT

FDA Adverse Event
Death ·CRYOLIFE, INC.·Product code MIE·December 29, 2021

*

FDA Adverse Event
Death ·CRYOLIFE INC·Product code MIE·February 17, 2002

LIFENET

FDA Adverse Event
Death ·LIFENET·Product code MIE·July 25, 2003